Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR Coexisting NRAS and BRAF mutations in primary familial melanomas with specific CDKN2A germline alterations. 19759551

2010
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A. 20340136

2010
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents. 16905682

2007
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR CDKN2A germline mutations in individuals with cutaneous malignant melanoma. 17218939

2007
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL. 17047042

2006
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR The prevalence of CDKN2A germ-line mutations and relative risk for cutaneous malignant melanoma: an international population-based study. 16896043

2006
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample. 16234564

2005
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR Familial melanoma, pancreatic cancer and germline CDKN2A mutations. 15146471

2004
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR Geographical variation in the penetrance of CDKN2A mutations for melanoma. 12072543

2002
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR Validation of denaturing high performance liquid chromatography as a rapid detection method for the identification of human INK4A gene mutations. 11687599

2001
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR CDKN2A variants in a population-based sample of Queensland families with melanoma. 10070944

1999
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR The p16INK4a/CDKN2A tumor suppressor and its relatives. 9823374

1998
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds. 9416844

1997
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR CDKN2A (p16INK4A) somatic and germline mutations. 8723678

1996
dbSNP: rs878853650
rs878853650
CDKN2A
G 0.700 GeneticVariation CLINVAR Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds. 8595405

1995